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C Stoll

Showing results (131-140 of 377) with videos related to

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Journal De Genetique Humaine|September 1, 1980
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome]C Stoll, M P Roth, J M Levy
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Wiedemann-Rautenstrauch syndrome. A case report and review of the literatureC Stoll, F Labay, J Geisert, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Familial cylindromatosisC Stoll, Y Alembik, A Wilk, et al.
Clinical Genetics|January 1, 1976
An unusual partial trisomy 13C Stoll, J Messer, S Weitzenblum, et al.
Archives Francaises De Pediatrie|October 1, 1988
[Radiologic case of the month. Pneumatocele on infected intrapulmonary hematoma]Y Alembik, L Donato, C Roy, et al.
Annales De Genetique|January 1, 1997
De novo trisomy 22 due to an extra 22Q-chromosomeC Stoll, P Medeiros, H Pécheur, et al.
Birth Defects Original Article Series|January 1, 1976
Usefulness of chromosome catalog in delineating new syndromesD S Borgaonkar, Y E Lacassie, C Stoll
Laryngo- Rhino- Otologie|July 27, 2000
[Speech improvement with velopharyngoplasty in patients with lip-jaw-palate clefts]C Stoll, M Hochmuth, M Merting, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|August 31, 2000
Refinement of velopharyngoplasty in patients with cleft palate by covering the pharyngeal flap with nasal mucosa from the velumC Stoll, M Hochmuth, P Meister, et al.
Advances in Experimental Medicine and Biology|February 23, 1999
The influence of CD44 splice variants to the outcome of patients with oral squamous cell carcinomaC Stoll, G Baretton, F Soost, et al.
Pageof 38

Showing results (131-140 of 377) with videos related to

Sort By:
Pageof 38
Journal De Genetique Humaine|September 1, 1980
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome]C Stoll, M P Roth, J M Levy
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Wiedemann-Rautenstrauch syndrome. A case report and review of the literatureC Stoll, F Labay, J Geisert, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Familial cylindromatosisC Stoll, Y Alembik, A Wilk, et al.
Clinical Genetics|January 1, 1976
An unusual partial trisomy 13C Stoll, J Messer, S Weitzenblum, et al.
Archives Francaises De Pediatrie|October 1, 1988
[Radiologic case of the month. Pneumatocele on infected intrapulmonary hematoma]Y Alembik, L Donato, C Roy, et al.
Annales De Genetique|January 1, 1997
De novo trisomy 22 due to an extra 22Q-chromosomeC Stoll, P Medeiros, H Pécheur, et al.
Birth Defects Original Article Series|January 1, 1976
Usefulness of chromosome catalog in delineating new syndromesD S Borgaonkar, Y E Lacassie, C Stoll
Laryngo- Rhino- Otologie|July 27, 2000
[Speech improvement with velopharyngoplasty in patients with lip-jaw-palate clefts]C Stoll, M Hochmuth, M Merting, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|August 31, 2000
Refinement of velopharyngoplasty in patients with cleft palate by covering the pharyngeal flap with nasal mucosa from the velumC Stoll, M Hochmuth, P Meister, et al.
Advances in Experimental Medicine and Biology|February 23, 1999
The influence of CD44 splice variants to the outcome of patients with oral squamous cell carcinomaC Stoll, G Baretton, F Soost, et al.
Pageof 38